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Elika Esmaeilzadeh-Gharehdaghi
Elika Esmaeilzadeh-Gharehdaghi
Tarbiat Modares University
Biology
Secretion
Reelin
Cell biology
Point mutation
5
Papers
15
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Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and AS
2020
European Journal of Human Genetics
Masoud Garshasbi
Mahdi Mahmoudi
Ehsan Razmara
Mahdi Vojdanian
Saeed Aslani
Elham Farhadi
LR Jensen
Seyed Masoud Arzaghi
Shiva Poursani
Amirreza Bitaraf
Milad Eidi
Elika Esmaeilzadeh-Gharehdaghi
Andreas W. Kuss
Ahmad Reza Jamshidi
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Whole‐exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis
2020
Molecular Genetics & Genomic Medicine
Ehsan Razmara
Homeyra Azimi
Amirreza Bitaraf
Mohammad Ali Daneshmand
Mohammad Galehdari
Maryam Dokhanchi
Elika Esmaeilzadeh-Gharehdaghi
Masoud Garshasbi
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Citations (5)
Functional Analysis of RELN S2486G Mutation and its Contribution to Pathogenesis of Ankylosing Spondylitis.
2020
Archives of Iranian Medicine
Elika Esmaeilzadeh-Gharehdaghi
Ehsan Razmara
Amirreza Bitaraf
Ahmadreza Jamshidi
Mahdi Mahmoudi
Masoud Garshasbi
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S3440P Substitution in C-Terminal Region of Human Reelin Dramatically Impairs Secretion of Reelin from HEK 293T Cells
2019
Elika Esmaeilzadeh-Gharehdaghi
Ehsan Razmara
Amirreza Bitaraf
Mahdi Mahmoudi
Masoud Garshasbi
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S3440P Substitution in C-Terminal Region of Human Reelin Dramatically Impairs Secretion of Reelin from HEK 293T Cells
2019
Cellular and Molecular Biology
Elika Esmaeilzadeh-Gharehdaghi
Ehsan Razmara
Amirreza Bitaraf
Mahdi Mahmoudi
Masoud Garshasbi
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Citations (6)
1